156329-85-0

• 

• Basic information

  1. Product Name: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-(fluorocarbonyl)-, methyl ester (9CI)
  2. Synonyms: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-(fluorocarbonyl)-, methyl ester (9CI)
  3. CAS NO:156329-85-0
  4. Molecular Formula: C8H9FO3
  5. Molecular Weight: 172.1536632
  6. EINECS: N/A
  7. Product Categories: ACIDHALIDE
  8. Mol File: 156329-85-0.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-(fluorocarbonyl)-, methyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-(fluorocarbonyl)-, methyl ester (9CI)(156329-85-0)
  11. EPA Substance Registry System: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-(fluorocarbonyl)-, methyl ester (9CI)(156329-85-0)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 156329-85-0(Hazardous Substances Data)

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156329-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156329-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156329-85:
(8*1)+(7*5)+(6*6)+(5*3)+(4*2)+(3*9)+(2*8)+(1*5)=150
150 % 10 = 0
So 156329-85-0 is a valid CAS Registry Number.

156329-85-0Upstream product

• 156329-69-0 2-thioxo-1,2-dihydropyridin-1-yl 3-(methoxycarbonyl)bicyclo<1.1.1>pentane-1-carboxylate 

156329-85-0Downstream Products

156329-85-0Relevant articles and documents

Synthesis of Some Bridgehead-Bridgehead-Disubstituted Bicyclopentanes

Della, Ernest W.,Taylor, Dennis K.

, p. 2986 - 2996 (2007/10/02)

The synthesis of a wide variety of 1,3-disubstituted bicyclopentanes is described, with particular emphasis on the generation of a series of 3-X-substituted bicyclopentyl bromides required for solvolytic studies.Functional group manipulation at the bridgehead was readily accomplished in the majority of cases by radical processes; in some instances, transformations were effected via carbanionic-type intermediates.

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